GLP inspection template
Audit types, including FDA mock audits, facility, process, or study audits, can differ widely among projects; however, all marketable products must undergo multiple audits for Good Laboratory Practices (GLP) compliance during their life cycle. Additionally, GLP compliance may require further inspections and/or audits by an independent auditor to bring your organization to compliance. This GLP inspection template can help you uniformly apply mock audits in your institute while having all aspects of edits covered in this template for optimal results.
This is an MS Word/pdf template of a checklist for a standard GLP inspection that you can use as a starting point for preparing for and/or conducting a GLP audit. We have saved this GLP inspection template in different formats (.pdf, .docx, .dotm, .dotx, .docm, .doc, and .dot) to ensure it is compatible with all systems.
Please note that in this GLP inspection template.
- The blank text placeholders in the form “_____________” indicate where you should insert specific detail (replace as appropriate).
- Replace all placeholders with project-specific information.
- Please review this template and feel free to adapt it to your specific needs.
- You have to use the logo of the Institution on this form.
- Leave the template version information in the lower left-hand corner of the documents.
Using this GLP inspection template and the instructions provided will assist you to:
- Qualify a contract test facility for GLP compliance.
- Make sure your preparation of an audit for GLP compliance will be consistent with ICH guidelines.
- Help auditors or QA/QC specialists include the required items in their audits.
- Verify that you performed your studies in a GLP-compliant manner.
Who Can Benefit From This GLP inspection template:
This GLP inspection template can assist the following in the preparation of audits for GLP compliance:
- Anybody interested in preparing for audits for GLP compliance
- Manufacturing & Production Personnel / Managers
- Research and Development Personnel (R&D) / Managers
- Quality Assurance/ Control Personnel / Managers
- Regulatory affairs personnel/managers
- Laboratory Personnel / Managers
- Clinical trial personnel
- Project Managers
- ID: 1790
- SKU: TE-0003-MQ
- Type: Template
- Format: Template File (.docx, .dotm, .dotx, .docm, .doc, and .dot)
- Date of Last Update: Aug 01, 2017
- Price: $100.00
- Firstly, upon Check out, check your basket to make sure you have the right products for your need.
- Secondly, fill out the billing information and enter the Coupon Code if you have one.
- Thirdly, press “Proceed to PayPal” to pay for your selected products in the basket.
- Then, you will be directed to PayPal for payment, where you can pay with credit (Visa, Master Card, American Express, and Discover) or debit card (You do not need a PayPal account).
- At this point, you will be redirected back to the website.
- Finally, the link to download the PDF version of the document will be sent to you in the e-mail you will receive upon your registration and payment.
- Also, provide your feedback to us to improve our products at Easy Global Training.
Moreover, browse our collaborator’s site (Neometrix Consulting Inc.).